2005 Volume 73 Issue 8 Pages 644-650
The anodic hydrogen electrode reaction was examined in the Lewis acidic 66.7-33.3 mole percent (m/o) aluminum chloride-1-ethyl-3-methylimidazolium chloride (AlCl3-EtMeImCl) ionic liquid and the LiCl-buffered neutral AlCl3-EtMeImCl ionic liquid containing LiAlH4. Raman spectroscopy experiments revealed that the Al2Cl7− anion in the acidic ionic liquid is directly involved in the dissolution of the LiAlH4. Electrochemical hydrogen generation was verified by gas chromatography and XRD for Pd and Ti electrodes polarized in the ionic liquid. The hydrogen electrode reaction was irreversible, i.e., it followed an EirCir mechanism in the 66.7 m/o ionic liquid at 298 K. However, it was quasireversible in the LiCl-buffered ionic liquid at 353 K and appeared to follow an EqrCir mechanism.